Canonical Allele Identifier: CA379092760

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774887C>A (hg19) ; chr11:g.1753657C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753657C>A , CM000673.2:g.1753657C>A	GRCh38
NC_000011.9:g.1774887C>A , CM000673.1:g.1774887C>A	GRCh37
NC_000011.8:g.1731463C>A	NCBI36
NG_008655.1:g.15336G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1085G>T MANE Select	ENSP00000236671.2:p.Gly362Val
ENST00000367196.4:c.980G>T	ENSP00000356164.4:p.Gly327Val
ENST00000427721.3:c.510G>T
ENST00000429746.2:c.980G>T	ENSP00000402586.2:p.Gly327Val
ENST00000433655.6:c.*251G>T	ENSP00000404902.1:n.*251G>T
ENST00000438213.6:c.1202G>T	ENSP00000415036.2:p.Gly401Val
ENST00000497544.3:n.793G>T
ENST00000636397.1:c.1071+146G>T	ENSP00000489910.1:n.1071+146G>T
ENST00000636571.1:c.1064G>T	ENSP00000490770.1:p.Gly355Val
ENST00000636579.1:c.72+146G>T	ENSP00000490489.1:n.72+146G>T
ENST00000636615.1:c.1071+146G>T	ENSP00000490014.1:n.1071+146G>T
ENST00000636843.1:c.1079G>T	ENSP00000490897.1:p.Gly360Val
ENST00000637158.1:n.683G>T
ENST00000637381.2:n.3513G>T
ENST00000637387.1:c.1064G>T	ENSP00000490598.1:p.Gly355Val
ENST00000637815.2:c.1067G>T	ENSP00000490344.1:p.Gly356Val
ENST00000637915.1:c.1076G>T	ENSP00000490471.1:p.Gly359Val
ENST00000637937.1:n.393G>T
ENST00000678991.1:c.*946G>T	ENSP00000503019.1:n.*946G>T
ENST00000236671.6:c.1085G>T	ENSP00000236671.2:p.Gly362Val
ENST00000427721.2:c.471+146G>T	ENSP00000415840.2:n.471+146G>T
ENST00000429746.1:c.416G>T	ENSP00000402586.1:p.Gly139Val
ENST00000433655.5:c.*251G>T	ENSP00000404902.1:n.*251G>T
NM_001909.4:c.1085G>T	NP_001900.1:p.Gly362Val
NM_001909.5:c.1085G>T MANE Select	NP_001900.1:p.Gly362Val